FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

GREATBATCH SCIENTIFIC MR COMPATIBLE ARTHROSCOPES AND SMALL JOINT ARTHROSCOPES

K Number: K971781 · Decision Nov 21, 1997
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
9
Review Days
191

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
GREATBATCH SCIENTIFIC MR COMPATIBLE ARTHROSCOPES AND SMALL JOINT ARTHROSCOPES
K Number
K971781
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Wilson Greatbatch Technologies, Inc.
Date Received
May 14, 1997
Decision Date
November 21, 1997
Product Code
HRX
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HRX Arthroscope

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HRX), ordered by most recent decision date.

View all

Other Clearances by Wilson Greatbatch Technologies, Inc.

K Number Device Name
K971374 GREATBATCH SCIENTIFIC MR COMPATIBLE HYSTEROSCOPE
K971377 GREATBATCH SCIENTIFIC MR COMPATIBLE LARYNGOSCOPE
K972280 GREATBATCH SCIENTIFIC MR COMPATIBLE LAPAROSCOPES AND OPERATING LAPAROSCOPES
K970619 GREATBATCH SCIENTIFIC MRI COMPATIBLE FIBER OPTIC LARYNGOSCOPE HANDLE
K971375 GREATBATCH SCIENTIFIC MR COMPATIBLE SINUSCOPE
K954649 WGL ENDOSCOPIC GRASPER W/DETACHABLE STRAP
K950063 WGL ENDOSCOPIC GRASPER*
K942168 WGL ENDOSCOPIC GRASPER